Other specified congenital malformation syndromes affecting multiple systems

MESH PheWeb

No definition available.

Endpoint definition

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FinnGen phenotype data

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 Q87

Cause of death: ICD-10 Q87

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

Q17_OTHER_SPECIFE_CONGEN_MALFO_SYNDR_AFFECTING_MULTIPLE_SYSTEMS

Extra metadata

Level in the ICD hierarchy 3

First used in FinnGen datafreeze DF4

Parent code in ICD-10 Q8

Name in latin Alia syndromata malformationum congenitarum specificata, systemata multa afficientia

Similar endpoints

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List of similar endpoints to Other specified congenital malformation syndromes affecting multiple systems based on the number of shared cases.

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Narrower endpoints:

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Summary Statistics

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Key figures

	All	Female	Male
Number of individuals	282	149	133
Unadjusted prevalence (%)	0.11	0.10	0.12
Mean age at first event (years)	26.20	26.37	26.00

Mortality

Follow-up	Absolute risk	HR [95% CI]	p	N
1998–2019	-	-	-	-
15 years	-	-	-	-
5 years	-	-	-	-
1 year	-	-	-	-

Correlations

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Index endpoint: Q17_OTHER_SPECIFE_CONGEN_MALFO_SYNDR_AFFECTING_MULTIPLE_SYSTEMS – Other specified congenital malformation syndromes affecting multiple systems
GWS hits: 1

Survival analyses between endpoints

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Plot

before Other specified congenital malformation syndromes affecting multiple systems
after Other specified congenital malformation syndromes affecting multiple systems

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Table

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Drugs most likely to be purchased after Other specified congenital malformation syndromes affecting multiple systems

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